Middleton, L T <br/><br/>
Congenital myasthenic syndrome. (CMS) type Ia. Clinical and genetic diversity.  [electronic resource] 

 -  Annals of the New York Academy of Sciences  May 1998 
 - 157-66 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0077-8923 
<br/><br/><label>Standard No.: </label>10.1111/j.1749-6632.1998.tb10922.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child<br/>Child, Preschool<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 17<br/>Electrodiagnosis<br/>Female<br/>Genes, Dominant<br/>Genes, Recessive<br/>Genetic Linkage<br/>Genetic Variation<br/>Humans<br/>Lod Score<br/>Male<br/>Microsatellite Repeats<br/>Middle Aged<br/>Myasthenia Gravis--congenital<br/>Pedigree<br/>Receptors, Cholinergic--deficiency<br/>Syndrome